Mec1 inhibitors constitute a distinctive class of chemical compounds that have garnered significant attention in the realms of molecular biology and cellular signaling. At their core, these inhibitors are designed to target a specific protein known as Mec1, which is a conserved serine/threonine protein kinase present in various eukaryotic organisms, ranging from yeast to humans. Mec1 holds a pivotal role as a central component within the DNA damage response pathway, acting as a critical sensor of DNA damage and replication stress. When cells encounter DNA damage, Mec1 becomes activated, instigating a complex signaling cascade that subsequently culminates in a range of cellular responses, including cell cycle arrest, DNA repair, or, in instances of irreparable damage, programmed cell death, known as apoptosis.
The development and study of Mec1 inhibitors have profoundly contributed to our comprehension of the intricate mechanisms governing DNA damage response and cell cycle regulation. These inhibitors are typically crafted as small molecules or compounds specifically engineered to interact with distinct regions of the Mec1 protein, thereby disrupting its kinase activity. By employing Mec1 inhibitors, researchers have gained the ability to dissect the precise functions of this kinase within cellular processes such as DNA repair, DNA replication, and cell cycle progression. Consequently, Mec1 inhibitors offer a powerful tool for unraveling the underlying molecular pathways linked to genome stability, DNA damage repair, and cellular responses to environmental stressors.
| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Caffeine | 58-08-2 | sc-202514 sc-202514A sc-202514B sc-202514C sc-202514D | 50 g 100 g 250 g 1 kg 5 kg | $33.00 $67.00 $97.00 $192.00 $775.00 | 13 | |
Caffeine is a well-known non-specific inhibitor of Mec1/ATR. It can interfere with the DNA damage response by preventing the activation of Mec1. | ||||||
VE 821 | 1232410-49-9 | sc-475878 | 10 mg | $360.00 | ||
VE-821 is a small molecule inhibitor that selectively targets ATR (Mec1) kinase activity. It has been used in research to study the DNA damage response pathway. | ||||||
Deoxyschizandrin | 61281-38-7 | sc-278925 | 10 mg | $80.00 | ||
Schisandrin B is a natural compound found in Schisandra chinensis. It has been shown to inhibit ATR/Mec1 activity and may have potential in cancer research. | ||||||
NU6027 | 220036-08-8 | sc-215591 | 10 mg | $156.00 | 1 | |
NU6027 is a selective and potent inhibitor of ATR (Mec1) kinase. It is often used in laboratory settings to investigate the role of ATR in DNA damage responses. | ||||||
Ceralasertib | 1352226-88-0 | sc-507439 | 10 mg | $573.00 | ||
AZD6738 is an ATR inhibitor that is being investigated in research models for its potential in cancer therapy. It can block the kinase activity of ATR (Mec1). | ||||||
ATM/ATR Kinase Inhibitor Inhibitor | 905973-89-9 | sc-202964 | 5 mg | $106.00 | 8 | |
CGK733 is a small molecule inhibitor of ATR (Mec1) that has been used to explore the DNA damage response pathway and its potential as a therapeutic target. | ||||||
XAV939 | 284028-89-3 | sc-296704 sc-296704A sc-296704B | 1 mg 5 mg 50 mg | $36.00 $117.00 $525.00 | 26 | |
XAV-939 is a compound that can inhibit ATR activity indirectly by affecting the stability of the protein. It is used in research to study ATR regulation. | ||||||
AZ20 | 1233339-22-4 | sc-503186 | 5 mg | $255.00 | 1 | |
AZ20 is a potent inhibitor of ATR that has been developed for research purposes. It can block ATR kinase activity and is used to investigate its role in DNA damage repair. | ||||||